Mineral composition, especially for use in paper fillers and paper or plastic coatings

ABSTRACT

A mineral composition comprising mineral particles, said mineral particles, when in a densely compacted bed form, having a volume defined median pore diameter from 0.01 to 0.04 micrometre, and having an intruded total specific void volume of 0.1-0.3 cm 3 /g. A specific advantage of this composition is that it as a component in a coating, allows the passage of ink solvent into the base paper while retaining the ink molecules on the surface.

CROSS-REFERENCE TO RELATED APPLICATIONS

This is a divisional of U.S. application Ser. No. 13/991,510, filed Jun. 4, 2013, which is a U.S. National Phase of PCT Application No. PCT/EP2011/072768, filed Dec. 14, 2011, which claims priority to European Application No. 10195360.2, filed Dec. 16, 2010, U.S. Provisional Application No. 61/425,339, filed Dec. 21, 2010, U.S. Provisional Application No. 61/452,981, filed Mar. 15, 2011 and U.S. Provisional Application No. 61/523,927, filed Aug. 16, 2011, the contents of which are hereby incorporated herein by reference in their entirety.

TECHNICAL FIELD OF THE INVENTION

The present invention relates to mineral compositions with high adsorptive capacity. In particular the present invention relates to printing paper fillers and coatings with high adsorptive capacity.

BACKGROUND OF THE INVENTION

Mineral fillers are used on a large scale in paper manufacturing. Their function consists primarily of increasing the opacity of the paper and level of brightness. Relatively inexpensive mineral fillers include china clay, natural calcium carbonate-such as ground calcium carbonate, precipitated calcium carbonate, talcum and calcium sulphates. In addition to optical properties, mineral fillers also influence weight, volume, porosity, mechanical properties, particularly bursting strength, the smoothness of the surface, and printing characteristics.

U.S. Pat. No. 5,292,365 discloses a single product which can be used equally as paper filler and as a coating pigment having

a) a rhombohedral or round particle shape b) a steepness factor (Particle diameter in micrometres at 50% of mass/Particle diameter in micrometres at 20% of mass (d₅₀/d₂₀) of between 1.1 and 1.4 c) a ratio R (volume mass % of particles <1 micrometres/volume mass % of particles <0.2 micrometres) of 8-19 and d) an average particle diameter of between 0.4 and 1.5 micrometres. The average particle diameter of the invented products is the particle diameter in microns, derived from the X-axis at a value on the Y-axis of 50% mass of the particles.

The top cut is between 4 and 7 micrometres. The term “top cut” refers to the size (in microns) of the coarsest particles of the product. For example, a top cut of 10 microns means that 100% of the particles are smaller than 10 microns. The inventors of the present invention will define the top cut by d₉₈ due to the fact that the 100% line is varying at least ±0.5% far up (error bar).

WO2009009553 discloses precipitated calcium carbonate compositions for coating exhibiting improved opacity, sheet gloss, print gloss, and brightness. The precipitated calcium carbonate compositions are characterized by having a crystalline aragonite content of greater than or equal to about 30% by weight relative to the total weight of the composition. Furthermore, less than or equal to about 10% by weight of particles are having a particle size less than or equal to about 0.25 micrometres. Less than or equal to about 4% by weight of particles have a particle size greater than or equal to about 2.0 micrometres, and a particle size distribution steepness factor ((d₃₀/d₇₀)*100) of greater than or equal to about 50.

US patent application 2006292305 discloses a composition with a first pigment component comprising particulate ground calcium carbonate (GCC) having a particle size distribution (psd) steepness factor ((d₃₀/d₇₀)*100) ranging from about 30 to about 45; and a second pigment component comprising particulate precipitated calcium carbonate (PCC) having a psd steepness factor ranging from about 55 to about 75 and a d₅₀ not greater than 0.5.

Canadian patent 1150908 discloses a calcium carbonate composition with a ratio R (% of particles<1 micrometres/% of particles <0.2 micrometres) greater than 3.5. EP 1 452 489 A1 discloses a material for imparting thixotropy, the material comprising surface-treated calcium carbonate. The surface-treated calcium carbonate has been prepared by treating a calcium carbonate with fatty acids, resin acids, such as abietic acid, dehydroabietic acid and dihydroabiteic acid; silane coupling agents such as vinylsilane, aminosilane and mercaptosilane; resins such as polyethylene, polypropylene and urethane resins; and polymeric dispersants.

SUMMARY OF THE INVENTION

While prior art has focused almost solely on particle sizes, the inventors of the present invention have found that mean pore diameter of the mineral composition is of outmost importance for optimal adsorption.

Surprisingly, it has been found by the inventors of the present invention that segregation of larger versus smaller particles during application, e.g. coating on different supports, can lead to different pore structure of the final coating. Hence, the pore structure cannot be controlled by the particle size distribution only.

Furthermore, segregation of large ink/dye molecules on the paper surface is aided by surface size exclusion and a high pore volume coating, allowing the passage of ink solvent into the base paper while retaining the ink molecules on the surface. This suggests the need for a porous coating formulation. One object of the present invention is therefore to introduce mineral compositions with a carefully controlled pore size distribution and capillarity.

Another object of the present invention is to introduce such optimal absorption of the ink solvent into the paper mass, by adding mineral compositions with a carefully controlled pore size distribution and capillarity as paper filler.

Thus, one aspect of the invention is to provide a mineral composition comprising mineral particles, said mineral particles, when in a densely compacted bed form, having a volume defined median pore diameter from 0.01 to 0.04 micrometre, and having an intruded total specific void volume of 0.1-0.3 cm³/g.

Another aspect of the present invention is to provide a mineral slurry for coating compositions, said slurry comprising mineral particles, said mineral particles, when in a densely compacted bed form, having a volume defined median pore diameter from 0.01 to 0.04 micrometre, and having an intruded total specific void volume of 0.1-0.3 cm³/g.

Yet another aspect of the present invention is to provide a coating composition comprising a mineral composition which comprises mineral particles, said mineral particles, when in a densely compacted bed form, having a volume defined median pore diameter from 0.01 to 0.04 micrometre, and having an intruded total specific void volume of 0.1-0.3 cm³/g.

Still another aspect of the present invention is to provide a filler for paper formulations, said filler comprising a mineral composition which comprises mineral particles, said mineral particles, when in a densely compacted bed form, having a volume defined median pore diameter from 0.01 to 0.04 micrometre, and having an intruded total specific void volume of 0.1-0.3 cm³/g.

Yet another aspect of the present invention is to provide a paper comprising a coating composition, said coating composition comprising a mineral composition which comprises mineral particles, said mineral particles, when in a densely compacted bed form, having a volume defined median pore diameter from 0.01 to 0.04 micrometre, and having an intruded total specific void volume of 0.1-0.3 cm³/g.

Another aspect of the present invention is to provide a paper comprising a filler, said filler comprising a mineral composition which comprises mineral particles, said mineral particles, when in a densely compacted bed form, having a volume defined median pore diameter from 0.01 to 0.04 micrometre, and having an intruded total specific void volume of 0.1-0.3 cm³/g.

One aspect of the present invention relates to a method for producing a mineral particle fine fraction from a feed material, the mineral particle fine fraction, when in a densely compacted bed form, having a volume defined median pore diameter from 0.01 to 0.04 micrometre, and having an intruded total specific void volume of 0.1-0.3 cm³/g, the method comprising:

-   -   providing the feed material to a milling machine, producing a         first milled feed material,     -   feeding the first milled feed material to a disc stack         centrifuge, producing two mineral particle fractions, one being         the mineral particle fine fraction and a second being a mineral         particle coarse fraction,     -   either feeding a part or all of the mineral particle coarse         fraction to a milling machine and/or to a disc stack centrifuge         and/or taking off a part or all of the mineral particle coarse         fraction.

Another aspect of the present invention relates to a method for producing a mineral particle fine fraction, the mineral particle fine fraction, when in a densely compacted bed form, having a volume defined median pore diameter from 0.01 to 0.04 micrometre, and having an intruded total specific void volume of 0.1-0.3 cm³/g, the method comprising:

-   -   providing the feed material to one or more dry and/or wet         grinding machines, producing said mineral particle fine fraction         in one or more grinding steps.

BRIEF DESCRIPTION OF THE FIGURES

FIG. 1 shows Mercury intrusion curves of the samples 1-7,

FIG. 2 shows pore size distribution curves of the samples 1-7, and

FIG. 3 shows an example of a process for producing the mineral particles of the present invention, and

FIG. 4 shows Tack Force Development curves of product coatings based on examples 3 and 6.

The present invention will now be described in more detail in the following.

DETAILED DESCRIPTION OF THE INVENTION

Both offset paper and inkjet paper have been manufactured with properties that counteract spreading of the ink and, hence, promote good printability. However, currently available multipurpose office papers are often associated with an unsatisfactory inkjet, rotogravure or offset print quality.

Thus, there exists a demand for coated multipurpose papers and in particular for papers suitable for inkjet, rotogravure or offset applications, which give an improved print quality without a corresponding increase in production cost.

It is known that a charge difference between adsorbent and adsorbate, respectively the paper surface and the dye molecules, is generally used to promote dye adsorption. If mineral particles are present in the coating formulation, the inherent adsorptive properties of mineral particles towards ink dyes can offer another alternative to reduce the quantity of cationic additives necessary to ensure a given optical density. While prior art has focused almost solely on particle sizes, the inventors of the present invention have found that mean pore diameter of the mineral composition is of outmost importance for optimal adsorption.

Segregation of large ink/dye molecules on the paper surface is aided by surface size exclusion and a high pore volume coating, allowing the passage of ink solvent into the base paper while retaining the ink molecules on the surface. This suggests the need for a porous coating formulation. One object of the present invention is therefore to introduce mineral compositions with a carefully controlled pore size distribution and capillarity.

In the present context, the term “capillarity” is to be understood as a phenomenon where the ink solvent spontaneously flows in the pores formed by the mineral particles.

As a representative test system to describe the mineral composition comprising mineral particles, a densely compacted bed is formed in a wet tablet press apparatus (Gane et al. 2000, Ridgway et al. 2004) from a water slurry of the mineral particles by applying a constant pressure (15 bars) to the suspension/slurry until the water is released by filtration through a fine 0.025 μm filter membrane. This method produces tablets of about 4 cm in diameter, with a thickness of 1.5-2.0 cm, which can be divided and fashioned into suitable sample configurations for subsequent analysis. The tablets were removed from the apparatus and dried in an oven at 60° C. for 24 hours. The representative test system is generally accepted and disclosed in (1) Ridgway, C. J., Gane P. A. C., Schoelkopf, J. (2004): “Modified Calcium Carbonate Coatings With Rapid Absorption and Extensive Liquid Uptake Capacity”, Colloids and Surfaces A, 236 (1-3), 91; (2) Gane, P. A. C., Kettle, J. P., Matthews, G. P. and Ridgway C. J. (1996): “Void Space Structure of Compressible Polymer Spheres and Consolidated Calcium Carbonate Paper-Coating Formulations”, Industrial & Engineering Chemistry Research Journal 35 (5), 1753-1764; (3) Gane, P. A. C., J. Schoelkopf, D. C. Spielmann, G. P. Matthews, C. J. Ridgway, Tappi J. 83 (2000) 77.

Portions of each tablet are characterized by mercury porosimetry for porosity, intruded total specific void volume, and pore size distribution using a Micromeritics Autopore IV mercury porosimeter. A mercury porosimetry experiment entails the evacuation of a porous sample to remove trapped gases, after which the sample is surrounded with mercury. The amount of mercury displaced by the sample allows calculation of the sample's bulk volume, V_(bulk). Pressure is then applied to the mercury so that it intrudes into the sample through pores connected to the external surface.

The maximum applied pressure of mercury was 414 MPa, equivalent to a Laplace throat diameter of 0.004 μm. The data is corrected using Pore-Comp for mercury and penetrometer effects, and also for sample compression. By taking the first derivative of the cumulative intrusion curves the pore size distributions based on equivalent Laplace diameter, inevitably including pore-shielding, are revealed. Volume defined median pore diameter is calculated from the Mercury intrusion curve, and FWHM is calculated from the pore size distribution curve.

In the present context, the term “intruded total specific void volume” is to be understood as the void volume measured by the above procedure (mercury porosimetry).

In the present context the term “mineral composition” will refer to a composition comprising mineral particles in the form of single particles, i.e. in a non-granular form. The term “mineral” refers to an element or chemical compound that is normally crystalline, such as calcium carbonate.

In the context of the present invention, the term “pore” is to be understood as describing the space that is found between the mineral particles, i.e. that is formed by the mineral particles and that allows the passage or absorption of fluids. The pores can be defined by their median pore diameter.

Another object of the present invention is to introduce such optimal absorption of the ink solvent into the paper mass, by adding mineral compositions with a carefully controlled pore size distribution and capillarity as paper filler.

In the present context the term “volume defined median pore diameter” will refer to the pore size, below which 50% of the specific pore volume is finer than this Young-Laplace equation defined equivalent capillary diameter, where the Young-Laplace equation is applied to the mercury intrusion porosimetry data (the above procedure).

Also, in the context of the present invention, the term “intruded total specific void volume” is to be understood as describing the measured pore volume (that is found between the mineral particles) per unit mass of mineral particles.

The present invention comprises the finding that improved properties, can be obtained when a substrate, such as paper, is coated with a coating composition which includes a mineral composition comprising mineral particles, said mineral particles, when in a densely compacted bed form, having a volume defined median pore diameter from 0.01 to 0.04 micrometre, and having an intruded total specific void volume of 0.1-0.3 cm³/g.

In the present context the term “substrate” is to be understood as any material having a surface suitable for printing or painting on, such as paper, cardboard, plastic, textile, wood, metal, concrete, or ointment.

In the present context, the term “plastic” relates to a natural or synthetic polymer material. Non limiting examples are polyethylene, polypropylene, polyvinylchloride, polyester, such as for example poly acrylic acid ester, homo or copolymers or mixtures thereof. The plastic may optionally be filled by a mineral filler, an organic pigment, an inorganic pigment or mixtures thereof.

In the present context, the term “textile” relates to a flexible material consisting of a network of natural or artificial fibres.

Thus, one aspect of the invention is to provide a mineral composition comprising mineral particles, said mineral particles, when in a densely compacted bed form, having a volume defined median pore diameter from 0.01 to 0.04 micrometre, and having an intruded total specific void volume of 0.1-0.3 cm³/g.

In one embodiment of the present invention, the volume defined median pore diameter is within a range from 0.01 micrometre to 0.039 micrometre, and having an intruded total specific void volume within a range from 0.10 cm³/g to 0.28 cm³/g; such as a volume defined median pore diameter within a range from 0.015 micrometre to 0.035 micrometre, and having an intruded total specific void volume within a range from 0.15 cm³/g to 0.27 cm³/g, e.g. a volume defined median pore diameter within a range from 0.017 micrometre to 0.033, and having an intruded total specific void volume within a range from 0.20 cm³/g to 0.25 cm³/g, such as a volume defined median pore diameter within a range from 0.019 micrometre to 0.030, and having an intruded total specific void volume within a range from 0.21 cm³/g to 0.24 cm³/g.

In another embodiment of the present invention, the volume defined median pore diameter is within a range from 0.013 micrometre to 0.038 micrometre, e.g. within a range from 0.018 micrometre to 0.036 micrometre, such as within a range from 0.021 micrometre to 0.034 micrometre, e.g. within a range from 0.023 micrometre to 0.028 micrometre.

In still another embodiment of the present invention, the intruded total specific void volume is within a range from 0.10 cm³/g to 0.29 cm³/g, e.g. within a range from 0.11 cm³/g to 0.28 cm³/g, such as within a range from 0.12 cm³/g to 0.27 cm³/g e.g. within a range from 0.13 cm³/g to 0.26 cm³/g, such as within a range from 0.14 cm³/g to 0.26 cm³/g, e.g. within a range from 0.15 cm³/g to 0.25 cm³/g, such as within a range from 0.16 cm³/g to 0.25 cm³/g, e.g. within a range from 0.17 cm³/g to 0.24 cm³/g, such as within a range from 0.18 cm³/g to 0.23 cm³/g, e.g. within a range from 0.19 cm³/g to 0.22 cm³/g, such as within a range from 0.20 cm³/g to 0.21 cm³/g.

The term “monomodal pore size distribution” as used herein refers to a collection of pores which have a single clearly discernable maxima on a pore size distribution curve (intensity on the ordinate or Y-axis, and pore size on the abscissa or X-axis). A bimodal pore size distribution refers to a collection of pores having two clearly discernable maxima on a pore size distribution curve. A generalised definition is, therefore, an n-modal pore size distribution referring to a collection of pores having n clearly discernable maxima on the pore size distribution curve, where n is an integer. The inventors of the present invention have found that one can obtain a better control of absorption speed through the mineral composition of multi viscous ink solvent mixtures when utilizing an n-modal pore size distribution, where n≧2 (higher than or equal to two).

The term “volume defined pore size polydispersity” is to be understood as a characteristic describing the breadth of distribution of pore size diameters to be found between the mineral particles. The inventors of the present invention have found that one can obtain a better control of absorption speed through the mineral composition when the volume defined pore size polydispersity, expressed as full width at maximum height (FWMH), is in the range of 0.01 to 0.03 micrometre.

A full width at half maximum (FWHM) is an expression of the extent of a function, given by the difference between the two extreme values of the independent variable at which the dependent variable is equal to half of its maximum value. The technical term Full-Width Half-Maximum, or FWHM, is used to approximate the diameter distribution of the majority of the pores, i.e. the polydispersity of the pore sizes. The inventors of the present invention have found that one can obtain a better control of speed of the ink solvent in the pores/capillaries when the pores are of uniform size compared to a broader size distribution.

In one embodiment of the present invention, the mineral particles, when in a densely compacted bed form, are having are monomodal pore diameter distribution and a volume defined pore size polydispersity expressed as full width at maximum height (FWMH) of less than, or equal to, 0.035 micrometre, such as within a range from 0.005 micrometre to 0.033 micrometre, e.g. 0.030 micrometre, such as from 0.01 micrometre to 0.028 micrometre, e.g. 0.025 micrometre, such as from 0.015 micrometre to 0.021 micrometre, e.g. 0.020 micrometre, such as from 0.016 micrometre to 0.019 micrometre.

In one embodiment of the present invention, the mineral particles, when in a densely compacted bed form, are having bimodal or multimodal pore diameter distribution.

In another embodiment of the present invention, the mineral particles, when in a densely compacted bed form, are having monomodal pore diameter distribution.

In still another embodiment of the present invention, the mineral particles comprise calcium carbonate, in particular chosen among natural calcium carbonate or precipitated calcium carbonate or their mixtures. Preferably, the mineral particles comprise calcium carbonate such as PCC (precipitated calcium carbonate), modified calcium carbonate (as notably in WO 00/39222, WO 2004/083316, WO 2005/121257) or GCC (ground calcium carbonate) and combinations thereof.

In the present context the term “mineral slurry” will refer to a particle suspension of the mineral composition in liquid, preferably water. Preferably, the mineral has a higher specific weight expressed in g/ml versus the liquid.

Another aspect of the present invention is to provide a mineral slurry for coating compositions, said slurry comprising mineral particles, said mineral particles, when in a densely compacted bed form, having a volume defined median pore diameter from 0.01 to 0.04 micrometre, and having an intruded total specific void volume of 0.1-0.3 cm³/g. Yet another aspect of the present invention is to provide a coating composition comprising a mineral composition which comprises mineral particles, said mineral particles, when in a densely compacted bed form, having a volume defined median pore diameter from 0.01 to 0.04 micrometre, and having an intruded total specific void volume of 0.1-0.3 cm³/g.

Still another aspect of the present invention is to provide a filler for paper formulations, said filler comprising a mineral composition which comprises mineral particles, said mineral particles, when in a densely compacted bed form, having a volume defined median pore diameter from 0.01 to 0.04 micrometre, and having an intruded total specific void volume of 0.1-0.3 cm³/g.

Yet another aspect of the present invention is to provide a paper comprising a coating composition, said coating composition comprising a mineral composition which comprises mineral particles, said mineral particles, when in a densely compacted bed form, having a volume defined median pore diameter from 0.01 to 0.04 micrometre, and having an intruded total specific void volume of 0.1-0.3 cm³/g.

Another aspect of the present invention is to provide a paper comprising a filler, said filler comprising a mineral composition which comprises mineral particles, said mineral particles, when in a densely compacted bed form, having a volume defined median pore diameter from 0.01 to 0.04 micrometre, and having an intruded total specific void volume of 0.1-0.3 cm³/g.

In another embodiment of the present invention, the formulation of the mineral composition is selected from the group consisting of a coating composition, filler, surface filling, and a mineral slurry, said mineral composition comprising mineral particles, said mineral particles, when in a densely compacted bed form, having a volume defined median pore diameter from 0.01 to 0.04 micrometre, and having an intruded total specific void volume of 0.1-0.3 cm³/g.

Another aspect of the present invention relates to a substrate comprising a mineral composition which comprises mineral particles, said mineral particles, when in a densely compacted bed form, having a volume defined median pore diameter from 0.01 to 0.04 micrometre, and having an intruded total specific void volume of 0.1-0.3 cm³/g.

In one embodiment of the present invention, the substrate comprises one or more formulations of the mineral composition, said formulation being selected from the group consisting of a coating composition, filler, surface filling, and a mineral slurry or mixtures thereof.

In another embodiment of the present invention, the substrate is selected from the group consisting of paper, cardboard, plastic, textile, wood, metal, concrete, or ointment.

One aspect of the present invention relates to the use of a mineral composition which comprises mineral particles, said mineral particles, when in a densely compacted bed form, having a volume defined median pore diameter from 0.01 to 0.04 micrometre, and having an intruded total specific void volume of 0.1-0.3 cm³/g in paper, cardboard, plastic, textile, wood, metal, concrete, or ointment.

Another aspect of the present invention relates to the use of a mineral composition which comprises mineral particles, said mineral particles, when in a densely compacted bed form, having a volume defined median pore diameter from 0.01 to 0.04 micrometre, and having an intruded total specific void volume of 0.1-0.3 cm³/g in paper application like paper manufacturing, paper coating, ink jet paper top-coating, offset printing.

Yet another aspect of the present invention relates to the use of a mineral composition which comprises mineral particles, said mineral particles, when in a densely compacted bed form, having a volume defined median pore diameter from 0.01 to 0.04 micrometre, and having an intruded total specific void volume of 0.1-0.3 cm³/g in textile and cardboard application.

In another embodiment of the present invention, the substrate comprises one or more blends of mineral particle compositions according to the present invention.

One aspect of the present invention relates to a method for producing a mineral particle fine fraction from a feed material, the mineral particle fine fraction, when in a densely compacted bed form, having a volume defined median pore diameter from 0.01 to 0.04 micrometre, and having an intruded total specific void volume of 0.1-0.3 cm³/g, the method comprising:

-   -   providing the feed material to a milling machine, producing a         first milled feed material,     -   feeding the first milled feed material to a disc stack         centrifuge, producing the two mineral particle fractions, one         being the mineral particle fine fraction and a second being a         mineral particle coarse fraction,     -   either feeding a part or all of the mineral particle coarse         fraction to a milling machine and/or to a disc stack centrifuge         and/or taking off a part or all of the mineral particle coarse         fraction.

In one embodiment of the present invention, the mineral particle coarse fraction, when in a densely compacted bed form, having a volume defined median pore diameter different from 0.01 to 0.04 micrometre, and having an intruded total specific void volume different from 0.1-0.3 cm³/g.

In another embodiment of the present invention, the mineral particle coarse fraction has a lower specific surface area (m²/g) than the mineral particle fine fraction, such as in the range of 0.1 to 100 times lower, e.g. 2 times lower, such as in the range of 5-95 times lower, e.g. 10 times lower, such as in the range of 15-85 times lower, e.g. 20 times lower, such as in the range of 25-75 times lower, e.g. 30 times lower, such as in the range of 35-65 times, e.g. 50 times lower than the mineral particle fine fraction.

In still another embodiment of the present invention, the feed material has a feed solids range of less than 99% by weight of the feed material, such as in the range of 5%-90%, e.g. 10%, preferably in the range of 15%-85%, e.g. 19%, such as in the range of 20%-80%, e.g. 25%, more preferably in the range of 30%-75%, e.g. 35%, such as in the range of 40%-70%, e.g. 45%, preferably in the range of 50%-65%, e.g. 55% by weight of the feed material.

A particular embodiment of the present invention is characterised in that the method for producing a mineral particle fine fraction, the mineral particle fine fraction, when in a densely compacted bed form, having a volume defined median pore diameter from 0.01 to 0.04 micrometre, and having an intruded total specific void volume of 0.1-0.3 cm³/g, comprises the following steps:

-   -   providing the feed material to a milling machine, producing a         first milled feed material,         -   feeding the first milled feed material into a disc stack             centrifuge, producing two mineral particle fractions, one             being the mineral particle fine fraction and a second being             a mineral particle coarse fraction,             wherein the first milled feed material has a solids contents             in the range of 20%-80% by weight, preferably in the range             of 30%-75% by weight, more preferably in the range of             38%-70% by weight.

The step of feeding the mineral particle coarse fraction to the disc stack centrifuge can in certain embodiments be repeated until that it is impossible or unfavourable to separate more mineral particle fine fraction from the mineral particle coarse fraction. The mineral fine fraction of a repeated feeding of the mineral particle coarse fraction to the disc stack centrifuge can be identical, coarser or finer than an earlier one. The different mineral particle fine fractions can be used separately or in blends of different mineral particle fine fractions.

Another aspect of the present invention relates to a method for producing a mineral particle fine fraction, the mineral particle fine fraction, when in a densely compacted bed form, having a volume defined median pore diameter from 0.01 to 0.04 micrometre, and having an intruded total specific void volume of 0.1-0.3 cm³/g, the method comprising:

providing the feed material to one or more dry and/or wet grinding machines, producing said mineral particle fine fraction in one or more grinding steps.

In one embodiment of the present invention, the process functions in a continuous manner.

An example of a method for producing the mineral particles of the present invention is shown in FIG. 3, where the feed material (1) is fed to a milling machine (6), producing a first milled feed material (3). The first milled feed material (3) is then fed to a disc stack centrifuge (7), producing the mineral particle fine fraction (4) and a mineral particle coarse fraction (2). The mineral particle coarse fraction (2) can be separated as a coarse fraction product (5), or fed back to the milling machine (6).

In one embodiment of the present invention, the mineral particle fine fraction, when in a densely compacted bed form, has a monomodal pore diameter distribution. In another embodiment of the present invention, the mineral particle fine fraction, when in a densely compacted bed form, has a volume defined pore size polydispersity expressed as full width at maximum height (FWMH) in the range of 0.01 to 0.03 micrometre.

In still another embodiment of the present invention, the mineral particle fine fraction, when in a densely compacted bed form, has a bi- or multimodal pore diameter distribution.

It should be noted that embodiments and features described in the context of one of the aspects of the present invention also apply to the other aspects of the invention.

All patent and non-patent references cited in the present application, are hereby incorporated by reference in their entirety.

The invention will now be described in further details in the following non-limiting examples.

EXAMPLES General Information to the Examples

All particle sizes and median diameters are measured using Malvern Mastersizer 2000 S, Malvern Instruments Ltd., Enigma Business Park, Grovewood Road, Malvern, Worcestershire, UK. WR14 1XZ using the following parameters:

PSD (particle size distribution) sample measurement procedure Prerequisites:

-   -   Instrument: Malvern Mastersizer 2000S with HydroS sampling unit.     -   ASTM Type II water is used as dilution water.     -   Malvern Mastersizer has been cleaned and has no contamination         from cationic charged material.     -   The instrument has been properly set-up and aligned.     -   The instrument is operated by an experienced and trained         operator.     -   A sample check standard on similar material to be measured has         been tested and validated prior to measurement.     -   Sample to be measured is fully homogenized.     -   Instrument Measurement options set to the following         -   Particle Refractive Index: 1.570         -   Particle Refractive Index blue light: 1.570         -   Dispersant Name: Water         -   Analysis model: General Purpose, irregular         -   Absorption: 0.005         -   Absorption blue light: 0.005         -   Dispersant Refractive Index: 1.330         -   Sensitivity: Normal         -   Size Range: 0.020-2000.000         -   Number of result bands: 66         -   Result Emulation: Not enabled         -   Result units: Microns         -   Background and background blue-light measurement time: 15             sec.         -   Test time: 15 sec

1.1. Equipment Preparation

-   -   1.1.1. Run Malvern through 3 cleaning cycles.     -   1.1.2. When cleaning cycles are complete, in the accessories         module, click on the “Empty” Button and allow the Hydro S to         drain.     -   1.1.3. When Hydro S is drained, close the drain valve by         clicking on the “Drain Valve” Button.     -   1.1.4. Slowly add ASTM Type II water into the hydro S until the         box next to “Liquid Sensed” becomes green.     -   1.1.5. Ramp pump speed to 3010 rpm. Maintain this speed during         measurement.     -   1.1.6. Continue to fill void with ASTM type II water.     -   1.1.7. Before pressing start, add a small amount (−1 ml) of −35%         concentration by weight of a sodium/calcium polyacrelate         dispersant having a molecular weight (Mw) of 5500 and a         polydispersity of 2.7 into the Hydro S sample unit.     -   1.1.8. Allow Dispersant to circulate for at least 1 minute         before adding sample to be measured.

1.2. Sample Measurement.

-   -   1.1. No Sonication to be used before or during sample         measurement.     -   1.2. When instrument is ready for measurement, add sample using         a 3 ml Syringe until an Obscuration of 13-25, preferably 20 is         attained.     -   1.3. When adding sample take care to not splash sample or do         anything else that may introduce air bubbles.     -   1.4. Start analysis.     -   1.5. In case of questionable results, run instrument check         standard to ensure that the instrument is running properly.

In Example 5 also a Sedigraph 5100 was use for the results given in weight %.

The BET specific surface area in m²/g is measured according to the standard ISO 4652 method (1994).

All weight, molecular weights (Mw), number molecular weights (Mn) and corresponding polydispersity of the different polymers are measured as 100 mol % sodium salt at pH 8 according to an aqueous Gel Permeation Chromatography (GPC) method calibrated with a series of five sodium polyacrylate standards supplied by Polymer Standard Service with references PSS-PAA 18 K, PSS-PAA 8K, PSS-PAA 5K, PSS-PAA 4K and PSS-PAA 3K.

Examples Representing Prior Art Example 1

By a hammer mill dry crushed and further dry ground and air cyclone-classified marble from the region of Villach, Austria, featuring a d₅₀ of 3.0 μm, a d₉₈ of 12.5 μm and a specific surface area of 2.3 m²/g. The dry grinding process in a ball mill using Silpex beads of 2.5 cm includes the use of 1000 ppm in respect to dry calcium carbonate of a triethanolamine-based dry grinding aid.

The fraction <2 μm was 30.3 volume %, and the fraction <1 μm was 5.6 volume %.

Example 2

Autogenic wet ground Vermont Marble, having a d₅₀ of 45 μm, is wet ground to a d₅₀ of 2.2 μm. The wet grinding is done at 78 weight % solids in tap water in a vertical attritor mill of a volume of 1500 liter in a continuous mode, using zircon silicate beads of 1-1.5 mm and using 0.63 wt % of a sodium/calcium polyacrylate dispersant having a molecular weight (Mw) of 5500 and polydispersity of 2.7. That means in total 0.70 weight % of sodium/calcium polyacrylate in respect to dry calcium carbonate. The final product further had a d₉₈ of 13.0 μm and a specific surface area of 6.0 m²/g. The fraction <2 μm was 46.3 volume %, and the fraction <1 μm was 22.6 volume %.

Example 3

The product of Example 2 was further wet ground using the same mill conditions as in Example 2 to a d₅₀ of 0.31 μm. The wet grinding is done at 72 weight % solids in tap water in a vertical attritor mill of a volume of 1500 liter in a continuous mode, using zircon silicate beads of 1-1.5 mm and using 0.42 wt % of a sodium/calcium polyacrylate dispersant having a molecular weight (Mw) of 5500 and polydispersity of 2.7. The final product further had a d₉₈ of 3.4 μm and a specific surface area of 10.5 m²/g. The fraction <2 μm was 87.7 volume %, and the fraction <1 μm was 60.3 volume %.

Examples Representing the Invention Example 4

The finely ground Marble of Example 2 was treated in a Westfalia “Teller-Düsen Separator” at feed solids of 38 weight % solids after dilution with tap water to reach a d₉₈ of 0.25 μm, d₉₀ of 0.20 μm and d₅₀ of 0.125 μm. The procedure was performed as described by Erich Müller, Mechanische Trennverfahren, Band 2, Otto Salle Verlag, Frankfurth, 1983, part 4.3 Zentrifugen in Tellerseparatoren page 65 ff, especially on page 78 Abb. 4.31.

Example 5

The finely ground Marble of Example 2 was treated in a Westfalia “Teller-Düsen Separator” at feed solids of 60.9 weight % solids after dilution with tap water to reach a d₉₈ of 0.225 μm and d₅₀ of 0.123 μm. The procedure was performed as described by Erich Müller, Mechanische Trennverfahren, Band 2, Otto Salle Verlag, Frankfurth, 1983, part 4.3 Zentrifugen in Tellerseparatoren page 65 ff, especially on page 78 Abb. 4.31.

Example 6

The finely ground Marble of Example 2 was treated in a Westfalia “Teller-Düsen Separator” at feed solids of 68.6 weight % solids after dilution with tap water to reach a d₉₈ of 0.295 μm and d₅₀ of 0.122 μm. The procedure was performed as described by Erich Müller, Mechanische Trennverfahren, Band 2, Otto Salle Verlag, Frankfurth, 1983, part 4.3 Zentrifugen in Tellerseparatoren page 65 ff, especially on page 78 Abb. 4.31.

Example 7

The product of Example 1 was made down into tap water to 75 weight % solids using 0.25 weight % of a sodium/calcium polyacrylate dispersant having a molecular weight (Mw) of 5500 and polydispersity of 2.7 and further wet ground using the same mill conditions as in Example 2 to a d₅₀ of 0.12 μm. The wet grinding is done at 45 weight % solids in tap water in a vertical attritor mill of a volume of 1500 liter in a continuous mode, using (Cermill) zircon silicate beads of less than 0.315 mm and using 1.4 wt % of a sodium/calcium polyacrylate dispersant having a molecular weight (Mw) of 5500 and polydispersity of 2.7. The final product further had a d₉₈ of 0.57 μm and a specific surface area of 35.8 m²/g. The fraction <0.5 μm was 97.5 volume % and fraction <0.1 μm was 37.5 volume %. The final product further had a d₉₀ of 0.90 μm.

The fraction less than 0.5 μm was 96 weight % and the fraction <0.2 μm was 71 weight % both measured by Sedimentation using a Sedigraph 5100, Micromeritics.

Example 8

The finely ground Marble of Example 3 was treated in a Westfalia “Teller-Düsen Separator” at feed solids of 38 weight % solids to reach a d₉₈ of 0.25 μm, d₉₀ of 0.2 μm and d₅₀ of 0.12 μm. The procedure was performed as described by Erich Müller, Mechanische Trennverfahren, Band 2, Otto Salle Verlag, Frankfurth, 1983, part 4.3 Zentrifugen in Tellerseparatoren page 65 ff, especially on page 78 Abb. 4.31 The fraction <0.5 μm was >99.5 volume %.

Example 9

50 tons of autogenic dry ground Canadian Marble (origin of the region of Perth) with a d₅₀ of 45 μm and originally a part of acid insoluble silicates and silica of 6.5 weight % was passing a froth flotation process to reduce the acid insol. part to >1 weight % by using 500 ppm in respect to total crude Marble, of tallow fatty imidazoline as silicate collector, is wet ground at 72 weight % solids in presence of 3.0 wt % of a sodium/magnesium polyacrylate dispersant (Mw of 5500, polydispersity of 2.7) in a batch mode in the same kind of an attritor mill as in Example 2 to a fineness until 99 weight % of the particles having a diameter less than 1 μm, 88 weight % of the particles having a diameter <0.5 μm, 69 weight % of the particles having a diameter <0.2 μm, and 28 weight % of the particles having a diameter <0.1 μm. Specific surface area was measured to 28.2 m2/g, (BET), d90 was 0.58 μm, and d₅₀ was 0.12 μm.

Results: Formation of a Densely Compacted Bed (Compacted Tablet)

As a representative test system to describe the mineral composition comprising mineral particles, a densely compacted bed is formed in a wet tablet press apparatus from a water slurry of the mineral particles by applying a constant pressure (15 bars) to the suspension/slurry until the water is released by filtration through a fine 0.025 μm filter membrane. This method produces tablets of about 4 cm in diameter, with a thickness of 1.5-2.0 cm, which can be divided and fashioned into suitable sample configurations for subsequent analysis. The tablets were removed from the apparatus and dried in an oven at 60° C. for 24 hours.

Portions of each tablet were characterized by mercury porosimetry for porosity, intruded total specific void volume, and pore size distribution using a Micromeritics Autopore IV mercury porosimeter. The maximum applied pressure of mercury was 414 MPa, equivalent to a Laplace throat diameter of 0.004 μm. The data is corrected using Pore-Comp for mercury and penetrometer effects, and also for sample compression. By taking the first derivative of the cumulative intrusion curves the pore size distributions based on equivalent Laplace diameter, inevitably including pore-shielding, are revealed. Volume defined median pore diameter is calculated from the Mercury intrusion curve, and FWHM is calculated from the pore size distribution curve (FIGS. 1 and 2).

TABLE 1 Collected data from the examples 1-9. Full-Width Half- Maximum (FWHM) pore size distribution/ μm Shows the degree of Intruded Volume defined uniformity of the Sample total specific median pore median pore size CaCO₃ void volume/cm³g⁻¹ diameter/μm diameter 1 0.292 0.50 0.440 2 0.114 0.09 0.067 3 0.140 0.06 0.051 4 0.271 0.04 0.026 7 0.211 0.02 0.019 8 0.258 0.03 0.022 9 0.150 0.02 0.018

Example 10 Use of the Product from Example 4 in an Inkjet Paper Top-Coating on a Porous Pre-Coat High Quality Inkjet Application Paper Pre-Coating

Paper Coater used: Erichsen K 303, Multicoater and corresponding rods for the equipment, both aviable at company Ericrson, D-58675 Hemen, Germany.

An inkjet base paper 112 g/m², Schoeller, Osnabrück, Germany, was pre-coated with 10 g/m² of the following formulation using rod N^(o) 3:

86.5 wt. % Omyajet B6606-FL 31% (modified calcium carbonate), Omya AG, Switzerland

4.5 wt. % PVA BF-05**

4.5 wt. % C-Film 05978, Cargill SA, Geneva (cationic starch)

4.5 wt. % Certrex, Mobil, (PolyDADMAC)

Coating colour solids was approximately 30 wt. %.

The coating was dried at 110° C. for 10 min. All wt. % are calculated dry on dry.

On top of this pre-coat the prior art or inventive product were applied using rods N^(o) 1 to 3.

Preparation of Top-Coating

The coating colours were run at similar binder amount and were diluted to approximately 25-30 weight % for good rheological properties and similar coat weight. The fumed silica* appeared to be somewhat difficult to apply on the paper at 30 weight % solids.

TABLE 2 Top-coating formulations of prior art and the present invention, Invention Prior art (wt % dry on dry) (wt % dry on dry) Product of Example 4 0 85.5 Aerodisp W 7330 N* 85.5 0 PVA BF-05** 14.5 14.5 Coating colour solids 25.3 30.2 *Aerosil ® fumed silica, Evonic, **98 mol % hydrolysed Polyvinylalcohol, low viscosity, ChangChun Groupe, South Korea.

Results Optical Print Density

TABLE 3 Optical density printed with Canon, OD Sum (/)*** Coat weight Coat weight 3 g/m² Coat weight 6 g/m² 10 g/m² Example 4 14 15 15 Prior art 11 13 14 ***Optical density Spectrolino ™, Spectrophotometer, Handhel system, GretagMacbeth ™ (OD sum = sum of cyan, magenta and yellow)

TABLE 4 Optical density printed with HP, OD Sum (/)*** Coat weight 6 g/m² Coat weight 10 g/m² Example 4 13.5 13.5 Prior art 12 11.5 ***Optical density Spectrolino ™, Spectrophotometer, Handhel system, GretagMacbeth ™ (OD sum = sum of cyan, magenta and yello)

Gloss

TABLE 5 uncalandered Paper gloss Uncalandered Tappi 75° (%) ISO Norm 8254-1 Coat weight 6 g/m² Coat weight 10 g/m² Example 4 43 52 Prior art 20 18

The present results show clearly the performance of inventive product of Example 4 versus fumed silica used as reference pigments.

The results indicate that the print density is improved versus fumed silica.

Furthermore, calcium carbonate products according to the present invention can be applied by using PVOH binder without rheological problems.

The gloss development of the carbonate products according to the present invention is more than two times better than commercial fumed silica references.

Example 11 Use of the Product from Example 3 and 8 in Offset Printing

Paper Coater used: Erichsen K 303, Multicoater, D-58675 Hemen, Germany.

A synthetic paper (YUPO Synteape, polypropylene, 62 g/m², 80 μm, halbmatt, weiss) Fischer Papier, 9015 St. Gallen, Switzerland) was coated with approximately 10 g/m² using rod N^(o) 2 and 45 g/m² using rod N^(o) 5 of the following formulation:

86.5 wt. % of product (either from example 3 or 8)

13.5 wt. % Styrene-Acrylate Binder (Acronal® S 360 D, BASF)

Coating colour solids was approximately 60 wt. %.

The coating was dried at 110° C. for 30 min. All wt. % are calculated dry on dry.

The resulting coat weights in m²/g were as follows:

Example 8 Example 3 Rod 2:  9.6 m²/g 10.9 m²/g Rod 5: 42.6 m²/g 45.0 m²/g

The results are the average of 3 measurements.

The tack force developments of the four coatings have been measured using the Ink Surface Interaction Tester (ISIT) to compare and evaluate their tack behaviour.

Ink-on-paper tack is measured by a special attachment (SeGan Ltd.) which consists of a solenoid, a coil spring, a load cell and a contact disc. The contact disc is pressed against the print on the sample platen by electromagnetic force acting on the solenoid. This action applies an extensional force on the coil spring mounted in parallel with the solenoid. Contact time and force can be varied by electronic controls to optimize adhesion between contact disc and print. At cessation of the electromagnetic force the contact disc is retracted from the print by the strain force of the extended coil spring, strong enough to achieve separation of the disc from the ink film. The strain gauge, fixed between contact disc and coil spring, generates a load-dependent signal which is recorded as the measured tack force. The sequence is automatically repeated for a predefined number of cycles chosen to span the regions of the tack force under study. The build-up of the tensile force required to achieve each individual separation is recorded with time and can be analyzed through specifically designed software. The maximum level of tensile force at each test point is plotted as measured tack force development with time.

The results (FIG. 4) show clearly that the tack force of the coating with the inventive product of Example 8 decreases to below 1 N in only 40 sec. After that period of time the printing is not sticky anymore, whereas the coating of the prior art product of Example 3 is not even back down after 150 sec and still sticky.

Example 12 Use of the Product from Example 7 in Recycled Board Topcoats

Three coating colours were formulated to compare the partial replacement of the titanium dioxide of the standard formulation by the calcium carbonate of example 7 according to the invention.

Coating Colour formulation n^(o) 1: Standard coating colour formulation

72.0 wt % Hydrafin Clay from Kamin LLC 8.0 wt % Calcined Clay Ansilex 93 from Engelhard

20.0 wt % Rutile TiO2

16 wt % latex P308 from Rohm & Haas 5 wt % protein binder Procote 200 from Protein Technologies International 0.7 wt % crosslinker ACZ 5800M from Akzo Nobel/Eka Chemicals 0.15 wt % polyacrylate dispersant Colloids 211 from Kemira Chemicals, Inc. Coating colour solids was approximately 43 wt %.

Coating Colour formulation n^(o) 2 according to the invention:

72.0 wt % Hydrafin Clay from Kamin LLC 8.0 wt % Calcined Clay Ansilex 93 from Engelhard

18.0 wt % Rutile TiO2

2.0 wt % calcium carbonate according to the example 7 16 wt % latex P308 from Rohm & Haas 5 wt % protein binder Procote 200 from Protein Technologies International 0.7 wt % crosslinker ACZ 5800M from Akzo Nobel/Eka Chemicals 0.15 wt % of polyacrylate dispersant Colloids 211 from Kemira Chemicals, Inc. Coating colour solids was approximately 43 wt %.

Coating Colour formulation n^(o) 3 according to the invention:

72.0 wt % Hydrafin Clay from Kamin LLC 8.0 wt % Calcined Clay Ansilex 93 from Engelhard

16.0 wt % Rutile TiO2

4.0 wt % calcium carbonate according to the example 7 16 wt % latex P308 from Rohm & Haas 5 wt % protein binder Procote 200 from Protein Technologies International 0.7 wt % crosslinker ACZ 5800M from Akzo Nobel/Eka Chemicals 0.15 wt % of polyacrylate dispersant Colloids 211 from Kemira Chemicals, Inc. Coating colour solids was approximately 43 wt %.

Coating Colour formulation n° 4 according to the invention:

70.2 wt % Hydrafin Clay from Kamin LLC 7.8 wt % Calcined Clay Ansilex 93 from Engelhard

16.0 wt % Rutile TiO2

8.0 wt % calcium carbonate according to the example 7 16 wt % latex P308 from Rohm & Haas 5 wt % protein binder Procote 200 from Protein Technologies International 0.7 wt % crosslinker ACZ 5800M from Akzo Nobel/Eka Chemicals 0.15 wt % of polyacrylate dispersant Colloids 211 from Kemira Chemicals, Inc. Coating colour solids was approximately 43 wt %.

Coating Colour formulation n^(o) 5 according to the invention:

72.0 wt % Hydrafin Clay from Kamin LLC 8.0 wt % Calcined Clay Ansilex 93 from Engelhard

14.0 wt % Rutile TiO2

6.0 wt % calcium carbonate according to the example 7 16 wt % latex P308 from Rohm & Haas 5 wt % protein binder Procote 200 from Protein Technologies International 0.7 wt % crosslinker ACZ 5800M from Akzo Nobel/Eka Chemicals 0.15 wt % of polyacrylate dispersant Colloids 211 from Kemira Chemicals, Inc. Coating colour solids was approximately 43 wt %.

Coating Colour formulation n^(o) 6 according to the invention:

72.0 wt % Hydrafin Clay from Kamin LLC 8.0 wt % Calcined Clay Ansilex 93 from Engelhard

12.0 wt % Rutile TiO2

8.0 wt % calcium carbonate according to the example 7 16 wt % latex P308 from Rohm & Haas 5 wt % protein binder Procote 200 from Protein Technologies International 0.7 wt % crosslinker ACZ 5800M from Akzo Nobel/Eka Chemicals 0.15 wt % of polyacrylate dispersant Colloids 211 from Kemira Chemicals, Inc. Coating colour solids was approximately 43 wt %.

(All wt % are calculated dry on dry of the total mineral materials).

Three top-coatings of a recycled cardboard were performed by applying on the cardboard sheet the dried coating weight of each of the formulations in the amount listed in Table 6 by using a RK Printcoat Instruments K Control Coater Model K202 with the following procedure:

-   1.1 The samples should be conditioned for a minimum of 24 hours at     TAPPI Standard Conditions (50%±2% Relative Humidity & 23° C.±1° or     73.4° F.±1.8°). -   1.2 Follow the instructions for setting up the instrument for     testing and calibrate the instrument as per the instructions. -   1.3 Place the conditioned samples sheets with the machine direction     of the board parallel to the face of the Brightimeter over the     sample opening on top of the instrument, place the 1 kg weight on     the sample and press the PRINT key for a single reading, or if an     average is required initiate the AVERAGE routine and follow the     instrument prompts. -   1.4 All the tests listed below can be accessed by programming the     instrument according to the directions in the manual. -   1.5 Do an average of ten (10) samples and record the     average±standard deviation.

Brightness Results

Brightness, when coated sample is placed over the black side of a Leneta FiberBoard from Leneta Company (Form N2C-2 B#3701 Unsealed Opacity Charts (194×260 mm) or 7⅝×10¼ inches) is determined according to the following method:

Drawdowns:

-   1. place the Leneta Board on the drawdown coater, holding it down     with the metal clamp (much like a clip board) -   2. place the proper size Meyer rod under the swing arms and on top     of the Leneta Board -   3. apply a bead of coating in front of the rod using a 10 cc or     larger syringe -   4. turn on the coater and flip the switch causing the rod to “draw     down” the length of the Leneta Board -   5. adjust the speed and rod size to achieve the desired coat weight     and film uniformity (may take several iterations) -   6. set aside the Meyer rod for cleaning and proceed to dry the     freshly coated Leneta Board

Drying

-   1. Using the heat gun (Veritemp Heat Gun Model VT-750C Master     Appliance Corp.), “blow” dry the Leneta Board while still in place     on the drawdown coater -   2. dry until the coating goes from a wet look to a dull, dry look -   3. turn on the felt drum dryer (Felt Roll Drum Dryer Adiron dack     Machine Corp.). -   4. then, using the felt drum dryer, place the Leneta Board coated     side against the drum (the goal of blow drying is to avoid any     sticking of this coating on the drum) -   5. with the felt drum drying turning, allow the Leneta Board to pass     in to the nip (between drum and felt) and wrap around to the other     side, where it comes out. -   6. place dried Leneta Board to the side for brightness testing or     coat weight determination

The results are given in the following Table 6.

TABLE 6 Brightness R457 TAPPI measured with Technidyne Corp. Brightimeter Micro S-5 Model S-5/BOC Serial # 452266. Standard Invention Invention Invention Invention Invention Formulation Formulation Formulation Formulation Formulation Formulation no 1 no 2 no 3 no 4 no 5 no 6 Brightness R457 TAPPI 69.3 77.0 75.9 76.6 74.7 73.3 Standard Deviation 1.2 0.6 0.6 0.6 0.6 0.6 Coating weight g/m² 3.1 3.2 3.2 3.4 3.3 3.3

The present results show clearly the performance of the product according to the invention. The results indicate that the brightness of a coated recycled board is improved by replacing a part of the titanium dioxide by the calcium carbonate according to the invention. Furthermore, calcium carbonate products according to the present invention can be applied without rheological problems. 

1. A method for producing a mineral particle fine fraction from a feed material comprising calcium carbonate, the method comprising: (i) milling the feed material in a milling machine to obtain a first milled feed material; (ii) subjecting the first milled feed material to a disc stack centrifuge to obtain a mineral particle fine fraction and a mineral particle coarse fraction; and (iii) either feeding a part or all of the mineral particle coarse fraction to a milling machine and/or to a disc stack centrifuge and/or taking off a part or all of the mineral particle coarse fraction, to obtain a mineral particle fine fraction comprising mineral particles comprising calcium carbonate, said mineral particles, when in a densely compacted bed form, have a volume defined median pore diameter from 0.01 to 0.04 micrometre, an intruded total specific void volume of 0.1 to 0.3 cm³/g, a monomodal pore diameter distribution, and a volume defined pore size polydispersity expressed as full width at maximum height (FWMH) in the range of 0.01 to 0.03 micrometre.
 2. The method according to claim 1, wherein said mineral particles, when in a densely compacted bed form, have a volume defined median pore diameter from 0.01 to 0.039 micrometre, and an intruded total specific void volume of 0.10 to 0.28 cm³/g.
 3. The method according to claim 1, wherein said mineral particles, when in a densely compacted bed form, have a volume defined median pore diameter from 0.015 to 0.035 micrometre, and an intruded total specific void volume of 0.15 to 0.27 cm³/g.
 4. The method according to claim 1, wherein said mineral particles, when in a densely compacted bed form, have a volume defined median pore diameter from 0.017 to 0.033 micrometre, and an intruded total specific void volume of 0.20 to 0.25 cm³/g.
 5. The method according to claim 1, wherein said mineral particles, when in a densely compacted bed form, have a volume defined median pore diameter from 0.019 to 0.030 micrometre, and an intruded total specific void volume of 0.21 to 0.24 cm³/g.
 6. The method according to claim 1, wherein said mineral particles, when in a densely compacted bed form, have a volume defined pore size polydispersity expressed as full width at maximum height (FWMH) in the range of 0.01 to 0.028 micrometre.
 7. The method according to claim 1, wherein said mineral particles, when in a densely compacted bed form, have a volume defined pore size polydispersity expressed as full width at maximum height (FWMH) in the range of 0.015 to 0.021 micrometre.
 8. The method according to claim 1, wherein said mineral particles, when in a densely compacted bed form, have a volume defined pore size polydispersity expressed as full width at maximum height (FWMH) in the range of 0.016 to 0.019 micrometre.
 9. The method according to claim 1, wherein the mineral particles comprise natural calcium carbonate, precipitated calcium carbonate, or a mixture thereof.
 10. The method according to claim 1, wherein the mineral particles comprise natural calcium carbonate.
 11. The method according to claim 1, wherein the first milled feed material has a solids contents in the range of 20%-80% by weight.
 12. The method according to claim 1, wherein the first milled feed material has a solids contents in the range of 30%-75% by weight.
 13. The method according to claim 1, wherein the first milled feed material has a solids contents in the range of 38%-70% by weight.
 14. The method according to claim 1, wherein in step (iii) the mineral particle coarse fraction is subjected to milling in one or more dry grinding and/or wet grinding machines to obtain the mineral particle fine fraction in one or more grinding steps.
 15. The method according to claim 1, which is performed in a continuous manner. 